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1E7-03, a low MW compound targeting host protein phosphatase-1, inhibits HIV-1 transcription.

British journal of pharmacology | 2014

HIV-1 transcription is activated by the Tat protein which recruits the cyclin-dependent kinase CDK9/cyclin T1 to TAR RNA. Tat binds to protein phosphatase-1 (PP1) through the Q(35) VCF(38) sequence and translocates PP1 to the nucleus. PP1 dephosphorylates CDK9 and activates HIV-1 transcription. We have synthesized a low MW compound 1H4, that targets PP1 and prevents HIV-1 Tat interaction with PP1 and inhibits HIV-1 gene transcription. Here, we report our further work with the 1H4-derived compounds and analysis of their mechanism of action.

Pubmed ID: 25073485 RIS Download

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: P30AI087714
  • Agency: NIAID NIH HHS, United States
    Id: P30 AI087714
  • Agency: NHLBI NIH HHS, United States
    Id: 1P50HL118006
  • Agency: NIAID NIH HHS, United States
    Id: U19AI109664-01
  • Agency: NCI NIH HHS, United States
    Id: P30 CA051008-16
  • Agency: NHLBI NIH HHS, United States
    Id: P50 HL118006
  • Agency: NCI NIH HHS, United States
    Id: P30 CA051008
  • Agency: NIGMS NIH HHS, United States
    Id: 1SC1GM082325
  • Agency: NCRR NIH HHS, United States
    Id: 2G12RR003048
  • Agency: NIAID NIH HHS, United States
    Id: U19 AI109664
  • Agency: NIGMS NIH HHS, United States
    Id: SC1 GM082325
  • Agency: NIMHD NIH HHS, United States
    Id: G12 MD007597
  • Agency: NCRR NIH HHS, United States
    Id: G12 RR003048

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